FDA Adverse Event Injury Summary report: N

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

MDR report key: 7626323 · Received June 21, 2018

Report

Report Number
2210968-2018-73638
Event Type
Injury
Date Received
June 21, 2018
Report Date
May 28, 2018
Manufacturer
ETHICON INC.
Product Code
GAW
PMA / PMN Number
K133356
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS REPORT IS RELATED TO A JOURNAL ARTICLE, THEREFORE NO PRODUCT WILL BE RETURNED FOR ANALYSIS AND THE BATCH HISTORY RECORDS CANNOT BE REVIEWED AS THE LOT NUMBER HAS NOT BEEN PROVIDED. CITATION: EYE (2011) 25, 735¿739; DOI:10.1038/EYE.2011.32 (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED IN JOURNAL ARTICLE TITLE: PROLENE FRONTALIS SUSPENSION IN PAEDIATRIC PTOSIS AUTHOR(S): K CHOW, N DEVA AND SGJ NG CITATION: EYE (2011) 25, 735¿739; DOI:10.1038/EYE.2011.32 THE AIM OF THIS RETROSPECTIVE CHART STUDY WAS TO ASSESS THE EFFICACY OF FRONTALIS SUSPENSION USING 4¿0 PROLENE SUTURES FOR PAEDIATRIC PTOSIS WITH POOR LEVATOR FUNCTION. FROM 2000 TO 2008, 23 PATIENTS (N=30 EYELIDS; N=13 MALE AND N=10 FEMALE; MEAN AGE ± SD OF 22.0±22.7 YEARS) WITH CONGENITAL MYOGENIC PTOSIS (N=17), BLEPHAROPHIMOSIS SYNDROME (N=5) AND MARCUS GUNN JAW-WINKING PTOSIS (N=1) UNDERWENT UNILATERAL OR BILATERAL FRONTALIS SUSPENSION SURGERY FOR PAEDIATRIC PTOSIS WITH POOR LEVATOR FUNCTION. IN THE PROCEDURE, A 4¿0 PROLENE SUTURE WAS PASSED TRANSVERSELY, PARTIAL THICKNESS, THROUGH THE UPPER LID TARSAL PLATE. THE NEEDLE OF THE PROLENE SUTURE WAS THEN REMOVED. POSTOPERATIVELY, ONE PATIENT DEVELOPED REDNESS ON ONE LID AFTER SURGERY AND WAS REGARDED AS A WOUND INFECTION WHICH WAS TREATED WITH ORAL ANTIBIOTICS, AND RESOLVED WITHIN A FEW DAYS WITHOUT LONG-TERM SEQUELAE. SUTURE EXTRUSION WAS NOT SEEN IN THE STUDY DUE TO BURYING PROLENE SUTURES WITHIN THE SUBCUTANEOUS TISSUES AND ITS LOW TISSUE REACTIVITY. PROLENE FRONTALIS SUSPENSION IS AN EFFECTIVE TECHNIQUE FOR THE TREATMENT OF PAEDIATRIC PTOSIS WITH POOR LEVATOR FUNCTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
469552 PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT SUTURE, NONABSORBABLE GAW ETHICON INC.

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention